rs17110563
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs17110563(C;T) |
Make rs17110563(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 71972526 |
Gene | TPH2 |
is a | snp |
is | mentioned by |
dbSNP | rs17110563 |
dbSNP (classic) | rs17110563 |
ClinGen | rs17110563 |
ebi | rs17110563 |
HLI | rs17110563 |
Exac | rs17110563 |
Gnomad | rs17110563 |
Varsome | rs17110563 |
LitVar | rs17110563 |
Map | rs17110563 |
PheGenI | rs17110563 |
Biobank | rs17110563 |
1000 genomes | rs17110563 |
hgdp | rs17110563 |
ensembl | rs17110563 |
geneview | rs17110563 |
scholar | rs17110563 |
rs17110563 | |
pharmgkb | rs17110563 |
gwascentral | rs17110563 |
openSNP | rs17110563 |
23andMe | rs17110563 |
SNPshot | rs17110563 |
SNPdbe | rs17110563 |
MSV3d | rs17110563 |
GWAS Ctlg | rs17110563 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs17110563, also known as Pro206Ser, is a SNP in the TPH2 gene. The minor allele of this SNP yielded an odds ratio of 4.8 (CI:1.6-14.8) for increased risk for bipolar disorder in a study of 883 Russian patients.[PMID 17905754]
ClinVar | |
---|---|
Risk | rs17110563(T;T) |
Alt | rs17110563(T;T) |
Reference | Rs17110563(C;C) |
Significance | Other |
Disease | Bipolar affective disorder |
Variation | info |
Gene | TPH2 |
CLNDBN | Bipolar affective disorder, susceptibility to |
Reversed | 0 |
HGVS | NC_000012.11:g.72366306C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000003314.2, |
[PMID 18797398] Investigation of the tryptophan hydroxylase 2 gene in bipolar I disorder in the Romanian population.